Global change drivers can interact in synergistic ways, yet the interactive effect of global change drivers, such as climatic warming and species invasions, on plant pollination are poorly represented in experimental studies. We paired manipulative experiments to probe two mechanistic pathways through which plant invasion and warming may alter phenology and reproduction of native plant species. In the first, we tested how experimental warming (+1.7°C) modulated flowering phenology and how this affected flowering overlap between a native plant (Dracophyllum subulatum) and an invasive plant (Calluna vulgaris L.). In the second experiment, we explored how variation in the ratio of native to invasive flowers, and the overall quantity of resources in a floral patch, affected the reproduction of the native species. We hypothesized that the flowering overlap of native and invasive plants would be altered by warming, given that invading plants typically exhibit greater phenological plasticity than native plants. Further, we hypothesized that pollination of native plant flowers would decrease in floral patches dominated by invasive plant flowers, but that this effect would depend on total floral density in the patch. As predicted, the invasive plant had a stronger phenological response to experimental warming than the native plant, resulting in increased flowering overlap between the native the invasive plants. There was a four‐fold increase in the number of native flowers co‐flowering with high densities of invasive flowers suggesting native plant competition for pollinators with invasive plants under a warmed climate. In the second experiment, we found depressed seed masses of the native species in high density floral patches that were dominated by invasive flowers relative to high density floral patches dominated by native flowers. At low floral densities, seed mass of native plants was unaffected by invasion. Together, these results demonstrate that by increasing their phenological overlap, warming may enhance the magnitude of existing competition for pollination exerted by an invasive plant on a native plant, particularly in plant patches with high floral density. Our results illustrate a novel pathway through which global change drivers can operate synergistically to alter an important ecosystem service: pollination.
Blue is a favored color of many humans. While blue skies and oceans are a common visual experience, this color is less frequently observed in flowers. We first review how blue has been important in human culture, and thus how our perception of blue has likely influenced the way of scientifically evaluating signals produced in nature, including approaches as disparate as Goethe’s Farbenlehre, Linneaus’ plant taxonomy, and current studies of plant-pollinator networks. We discuss the fact that most animals, however, have different vision to humans; for example, bee pollinators have trichromatic vision based on UV-, Blue-, and Green-sensitive photoreceptors with innate preferences for predominantly short-wavelength reflecting colors, including what we perceive as blue. The subsequent evolution of blue flowers may be driven by increased competition for pollinators, both because of a harsher environment (as at high altitude) or from high diversity and density of flowering plants (as in nutrient-rich meadows). The adaptive value of blue flowers should also be reinforced by nutrient richness or other factors, abiotic and biotic, that may reduce extra costs of blue-pigments synthesis. We thus provide new perspectives emphasizing that, while humans view blue as a less frequently evolved color in nature, to understand signaling, it is essential to employ models of biologically relevant observers. By doing so, we conclude that short wavelength reflecting blue flowers are indeed frequent in nature when considering the color vision and preferences of bees.
1. Climate warming is shifting the distributions of mountain plant species to higher elevations. Cold-adapted plant species are under increasing pressure from novel competitors that are encroaching from lower elevations. Plant capacity to adjust to these pressures may be measurable as variation in trait values within a species. In particular, the strength and patterns of intraspecific trait variation along abiotic and biotic gradients can inform us whether and how species can adjust their anatomy and morphology to persist in a changing environment.2. Here, we tested whether species specialized to high elevations or with narrow elevational ranges show more conservative (i.e. less variable) trait responses across their elevational distribution, or in response to neighbours, than species from lower elevations or with wider elevational ranges. We did so by studying intraspecific trait variation of 66 species along 40 elevational gradients in four countries in both hemispheres. As an indication of potential neighbour interactions that could drive trait variation, we also analysed plant species' height ratio, its height relative to its nearest neighbour.
<p>Drivers of global change have direct impacts on the structure of communities and functioning of ecosystems, and interactions between drivers may buffer or exacerbate these direct effects. Interactions among drivers can lead to complex non-linear outcomes for ecosystems, communities and species, but are infrequently quantified. Through a combination of experimental, observational and modelling approaches, I address critical gaps in our understanding of the interactive effects of climate change and plant invasion, using Tongariro National Park (TNP; New Zealand) as a model. TNP is an alpine ecosystem of cultural significance which hosts a unique flora with high rates of endemism. TNP is invaded by the perennial shrub Calluna vulgaris (L.) Hull. My objectives were to: 1) determine whether species-specific phenological shifts have the potential to alter the reproductive capacity of native plants in landscapes affected by invasion; 2) determine whether the effect of invasion intensity on the Species Area Relationship (SAR) of native alpine plant species is influenced by environmental stress; 3) develop a novel modelling framework that would account for density-dependent competitive interactions between native species and C. vulgaris and implement it to determine the combined risk of climate change and plant invasion on the distribution of native plant species; and 4) explore the possible mechanisms leading to a discrepancy in C. vulgaris invasion success on the North and South Islands of New Zealand. I show that species-specific phenological responses to climate warming increase the flowering overlap between a native and an invasive plant. I then show that competition for pollination with the invader decreases the sexual reproduction of the native in some landscapes. I therefore illustrate a previously undescribed interaction between climate warming and plant invasion where the effects of competition for pollination with an invader on the sexual reproduction of the native may be exacerbated by climate warming. Furthermore, I describe a previously unknown pattern of changing invasive plant impact on SAR along an environmental stress gradient. Namely, I demonstrate that interactions between an invasive plant and local native plant species richness become increasingly facilitative along elevational gradients and that the strength of plant interactions is dependent on invader biomass. I then show that the consequences of changing plant interactions at a local scale for the slope of SAR is dependent on the pervasion of the invader. Next, I demonstrate that the inclusion of invasive species density data in distribution models for a native plant leads to greater reductions in predicted native plant distribution and density under future climate change scenarios relative to models based on climate suitability alone. Finally, I find no evidence for large-scale climatic, edaphic, and vegetative limitations to invasion by C. vulgaris on either the North and South Islands of New Zealand. Instead, my results suggest that discrepancies in invasive spread between islands may be driven by human activity: C. vulgaris is associated with the same levels of human disturbance on both islands despite differences in the presence of these conditions between then islands. Altogether, these results show that interactive effects between drivers on biodiversity and ecosystem dynamics are frequently not additive or linear. Therefore, accurate predictions of global change impacts on community structure and ecosystems function require experiments and models which include of interactions among drivers such as climate change and species invasion. These results are pertinent to effective conservation management as most landscapes are concurrently affected by multiple drivers of global environmental change.</p>
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